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1-Bromonaphthalene

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1-Bromonaphthalene manufacturers

  • 1-Bromonaphthalene
  • 1-Bromonaphthalene pictures
  • $15.00
  • 2026-09-11
  • CAS:90-11-9
  • Min. Order: 1KG
  • Purity: 99%
  • Supply Ability: 200 tons/ year
  • 1-Bromonaphthalene
  • 1-Bromonaphthalene pictures
  • $200.00
  • 2026-09-02
  • CAS:90-11-9
  • Min. Order: 1KG
  • Purity: 99%, 99.5% Sublimated
  • 1-Bromonaphthalene
  • 1-Bromonaphthalene pictures
  • $10.70
  • 2026-05-28
  • CAS:90-11-9
  • Min. Order: 10kg
  • Purity: 99%
  • Supply Ability: 10000kg
1-Bromonaphthalene Basic information
Product Name:1-Bromonaphthalene
Synonyms:1-bromo-naphthalen;1-Naphthyl bromide;A-BROMONAPHTHALENE;ALPHA-BROMONAPHTHALENE;ALPHA-MONOBROMONAPHTHALENE;ALPHA-NAPHTHYL BROMIDE;1-BROMONAPHTHALENE;1-BROMO NAPTHALENE
CAS:90-11-9
MF:C10H7Br
MW:207.07
EINECS:201-965-2
Product Categories:Naphthalene series;Pyridines ,Heterocyclic Acids;C9 to C12;Chemical Synthesis;Halogenated Hydrocarbons;Organic Building Blocks;Building Blocks;Naphthalene derivatives;Aryl;C9 to C12;Halogenated Hydrocarbons;Aromatic Compounds;bc0001;90-11-9
Mol File:90-11-9.mol
1-Bromonaphthalene Structure
1-Bromonaphthalene Chemical Properties
Melting point −2-−1 °C(lit.)
Boiling point 133-134 °C10 mm Hg(lit.)
density 1.48 g/mL at 20 °C(lit.)
vapor pressure 0.013 hPa (20 °C)
refractive index n20/D 1.6570(lit.)
Fp >230 °F
storage temp. Store below +30°C.
solubility H2O: slightly soluble
form Liquid
color slightly yellow to deep brownish-yellow
Water Solubility slightly soluble
Thermal Conductivity0.11 W/(m·K) at 25 ℃
Merck 14,1425
BRN 1906414
Henry's Law Constant3.5×10-2 mol/(m3Pa) at 25℃, Duchowicz et al. (2020)
Dielectric constant5.1(19℃)
InChI1S/C10H7Br/c11-10-7-3-5-8-4-1-2-6-9(8)10/h1-7H
InChIKeyDLKQHBOKULLWDQ-UHFFFAOYSA-N
SMILESBrc1cccc2ccccc12
LogP4.06
Surface tension44.4mN/m at 20°C
CAS DataBase Reference90-11-9(CAS DataBase Reference)
NIST Chemistry ReferenceNaphthalene, 1-bromo-(90-11-9)
EPA Substance Registry SystemNaphthalene, 1-bromo- (90-11-9)
Safety Information
Hazard Codes Xn,Xi
Risk Statements 22-36-36/37/38-20/21/22
Safety Statements 26-36
RIDADR 2810
WGK Germany 3
RTECS QJ1545000
8
TSCA TSCA listed
HazardClass 6.1(b)
PackingGroup III
HS Code 29036990
Storage Class10 - Combustible liquids
Hazard ClassificationsAcute Tox. 4 Oral
Aquatic Acute 1
Aquatic Chronic 1
Eye Irrit. 2
ToxicityLD50 orally in Rabbit: 810 mg/kg
MSDS Information
ProviderLanguage
alpha-Bromonaphthalene English
ACROS English
SigmaAldrich English
ALFA English
1-Bromonaphthalene Usage And Synthesis
Chemical PropertiesThick colorless yellow to yellow-brown liquid with a pungent odor. Insoluble in water, miscible with alcohol, ether, benzene and chloroform. 1-Bromonaphthalene is one of two isomeric bromonaphthalenes, the other being 2-bromonaphthalene.
Uses1-Bromonaphthalene is used in organic synthesis and refractometry of fats. It is used in the preparation of N-aryl imidazoles and diaryl ethers. It is used to determine the refractive index of crystals and the water content of alcohols. It is utilized in the preparation of glutathione peroxidase-like antioxidant activity of diaryl diselenides. Further, it serves as a solvent for the exfoliation and dispersion of hexabenzocoronene. In addition to this, it is used as a refrigerant and a solvent molecular weight substance.
Preparation1-Bromonaphthalene is synthesized by the reaction of naphthalene with bromine: C10H8+ Br2→ C10H7Br + HBr.
Reaction: add carbon tetrachloride and naphthalene in the reaction pot, stirring and heating, and slowly add bromine at 45℃. After adding, keep the reaction at 70-80℃ for 3-4h. distillation to recover carbon tetrachloride, wash the reaction product, distill under reduced pressure, wash again, filter, dry and get the finished product.
Application1-Bromonaphthalene is a bromoarene that can be used in:
Palladium-catalyzed Suzuki–Miyaura coupling reaction with potassium aryltrifluoroborates without the use of phase-transfer catalysts or phosphine ligands.
The preparation of indeno annelated polycyclic aromatic hydrocarbons by reacting with o-bromobenzeneboronic acid and oligocyclic bromoarenes via Suzuki-Heck type coupling.
Ni catalyzed Kumada–Tamao–Corriu cross-coupling reaction with PhMgBr.
The preparation of arylnaphthalenes via palladium-catalyzed Suzuki-Miyaura cross-coupling reaction with aryl boronic acid.
Synthesis Reference(s)Organic Syntheses, Coll. Vol. 1, p. 121, 1941
Tetrahedron, 64, p. 4999, 2008 DOI: 10.1016/j.tet.2008.03.085
General DescriptionThe vibrational spectra of 1-bromonaphthalene has been studied.
Purification MethodsPurify 1-bromonaphthalene by passage through activated alumina, and three vacuum distillations. [Beilstein 5 H 547, 5 IV 1665.]
Tag:1-Bromonaphthalene(90-11-9) Related Product Information
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